Surrogate endpoints for the treatment of venous leg ulcers

被引:116
作者
Gelfand, JM
Hoffstad, O
Margolis, DJ
机构
[1] Univ Penn, Dept Dermatol, Philadelphia, PA 19104 USA
[2] Univ Penn, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
关键词
epidemiologic; leg ulcer; outcome assessment; randomized controlled trials; varicose ulcer;
D O I
10.1046/j.1523-1747.2002.19629.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Surrogate markers are endpoints that occur early in the course of treatment and are intended to predict the true, meaningful clinical endpoint. Surrogate markers have been used to study treatments for a wide range of diseases in which the true outcome is delayed. The evaluation of therapies for venous leg ulcers is challenged by the prolonged observation period necessary to reach the endpoint of healing. We have performed a large cohort study to examine wound healing characteristics as candidate surrogate markers of venous leg ulcer healing using the Curative Health Services population. A total of 58,038 wounds met our definition of venous leg ulcer; however, 1550 wounds were excluded based on size, depth, site, and/or involvement of tendon or bone, leaving 56,488 wounds in 29,189 patients for analysis. The median wound size was 189 mm(2) , with a median wound duration of 3 mo. Using a large cohort of diverse venous leg ulcer patients, we demonstrate that after only 4 wk of treatment the wound parameters log healing rate, log wound area ratio, and percentage change in wound area can be valid surrogate markers of healing at 12 or 24 wk of care. Based on the area under the receiver operator characteristic curve log rate, log area ratio, and percentage change in area can discriminate which patients will heal at 12 or 24 wk of care (receiver operator characteristic 0.72-0.80). These surrogates were further validated by demonstrating that established risk factors for not healing such as wound size and wound duration are also important risk factors for not achieving the surrogate endpoint. These surrogate markers for venous leg ulcer healing may allow for early clinical trials to be more efficient, and can allow clinicians to identify patients unlikely to heal early in the course of treatment in order to expedite referral to specialty centers or for the selection of stepped treatment algorithms.
引用
收藏
页码:1420 / 1425
页数:6
相关论文
共 34 条
[1]  
[Anonymous], 1990, WOUNDS
[2]  
Buyse M, 2000, DRUG INF J, V34, P447, DOI 10.1177/009286150003400213
[3]   Considerations in the evaluation of surrogate endpoints in clinical trials: Summary of a National Institutes of Health Workshop [J].
De Gruttola, VG ;
Clax, P ;
DeMets, DL ;
Downing, GJ ;
Ellenberg, SS ;
Friedman, L ;
Gail, MH ;
Prentice, R ;
Wittes, J ;
Zeger, SL .
CONTROLLED CLINICAL TRIALS, 2001, 22 (05) :485-502
[4]  
DOUCETTE MM, 1989, ARCH PHYS MED REHAB, V70, P780
[5]   Surrogate endpoints: the debate goes on [J].
Ellenberg, SS .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2001, 10 (06) :493-496
[6]  
*FDA ICH, 1998, FDA GOV SEP
[7]  
FDA Wound Healing Clin Focus Grp, 2001, WOUND REPAIR REGEN, V9, P258
[8]   Surrogate end points in clinical trials: Are we being misled? [J].
Fleming, TR ;
DeMets, DL .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (07) :605-613
[9]   STATISTICAL VALIDATION OF INTERMEDIATE END-POINTS FOR CHRONIC DISEASES [J].
FREEDMAN, LS ;
GRAUBARD, BI ;
SCHATZKIN, A .
STATISTICS IN MEDICINE, 1992, 11 (02) :167-178
[10]  
Fylling C P, 1989, J Enterostomal Ther, V16, P247